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O-Methylhydroxylamine hydrochloride → 1-Metyl-3-methoxyiminomethyl-4-(3,4-dichlorophenyl)piperidine

HRID 843267
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인쇄 미리보기

반응식

HRID 843267 반응식
[CH3:1][N:2]1[CH2:7][CH2:6][CH:5]([C:8]2[CH:13]=[CH:12][C:11]([Cl:14])=[C:10]([Cl:15])[CH:9]=2)[CH:4]([CH:16]=O)[CH2:3]1.Cl.[O:19]([NH2:21])[CH3:20]>C(O)(C)C>[CH3:1][N:2]1[CH2:7][CH2:6][CH:5]([C:8]2[CH:13]=[CH:12][C:11]([Cl:14])=[C:10]([Cl:15])[CH:9]=2)[CH:4]([CH:16]=[N:21][O:19][CH3:20])[CH2:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 521874O-Methylhydroxylamine hydrochlorideHCID 22617036HCID 22617036, 화합물

생성물 1

HCID 850740351-Metyl-3-methoxyiminomethyl-4-(3,4-dichlorophenyl)piperidine수율 40.2%

시약·촉매·용매 1

HCID 3776Isopropanol용매

실험 절차

To a solution of 1-methyl-3-formyl-4-(3,4-dichlorophenyl)piperidine (10 g, 33 mmol) in warm isopropanol (100 mL) was added methoxylamine hydrochloride (3 g, 36 mmol). The reaction was heated at reflux for 30 min. The solvent was evaporated off and the residue made basic (pH=9) using concentrated ammonia. Extraction with ether afforded 8.5 g of crude product. Purification by repeated column chromatography on silica using EtOAc/Et3N (95:5) as eleuent afforded 4 g of the title compound as an oil.

후처리

  1. temperatureThe reaction was heated
  2. temperatureat reflux for 30 min
  3. customThe solvent was evaporated off
  4. extractionExtraction with ether
  5. customafforded 8.5 g of crude product
  6. customPurification

출처 및 근거

ORD 기록
ord-ae17b915266a403fbfa97832321d1d04
출처 데이터셋
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06376673B1

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